Incidental Mutation 'R5073:Wdr17'
ID |
388979 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Wdr17
|
Ensembl Gene |
ENSMUSG00000039375 |
Gene Name |
WD repeat domain 17 |
Synonyms |
B230207L18Rik, 3010002I12Rik |
MMRRC Submission |
042662-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R5073 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
55082316-55180014 bp(-) (GRCm39) |
Type of Mutation |
critical splice acceptor site |
DNA Base Change (assembly) |
T to A
at 55143271 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000135805
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000127511]
[ENSMUST00000127511]
[ENSMUST00000129132]
[ENSMUST00000129132]
[ENSMUST00000144482]
[ENSMUST00000144711]
[ENSMUST00000144711]
[ENSMUST00000150488]
[ENSMUST00000150488]
[ENSMUST00000175915]
[ENSMUST00000175915]
[ENSMUST00000176866]
|
AlphaFold |
E9Q271 |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126316
|
Predicted Effect |
probably null
Transcript: ENSMUST00000127511
|
SMART Domains |
Protein: ENSMUSP00000115550 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
72 |
112 |
8.55e-8 |
SMART |
WD40
|
162 |
202 |
1.58e2 |
SMART |
WD40
|
205 |
252 |
4.26e1 |
SMART |
WD40
|
255 |
298 |
1.15e0 |
SMART |
WD40
|
383 |
422 |
1.59e-7 |
SMART |
WD40
|
425 |
465 |
2.39e0 |
SMART |
WD40
|
468 |
509 |
5.52e-2 |
SMART |
WD40
|
511 |
550 |
4.14e-6 |
SMART |
WD40
|
555 |
595 |
5.14e-11 |
SMART |
WD40
|
598 |
638 |
6.58e-9 |
SMART |
WD40
|
641 |
681 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000127511
|
SMART Domains |
Protein: ENSMUSP00000115550 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
72 |
112 |
8.55e-8 |
SMART |
WD40
|
162 |
202 |
1.58e2 |
SMART |
WD40
|
205 |
252 |
4.26e1 |
SMART |
WD40
|
255 |
298 |
1.15e0 |
SMART |
WD40
|
383 |
422 |
1.59e-7 |
SMART |
WD40
|
425 |
465 |
2.39e0 |
SMART |
WD40
|
468 |
509 |
5.52e-2 |
SMART |
WD40
|
511 |
550 |
4.14e-6 |
SMART |
WD40
|
555 |
595 |
5.14e-11 |
SMART |
WD40
|
598 |
638 |
6.58e-9 |
SMART |
WD40
|
641 |
681 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000129132
|
SMART Domains |
Protein: ENSMUSP00000134935 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
48 |
88 |
8.55e-8 |
SMART |
Blast:WD40
|
91 |
131 |
1e-12 |
BLAST |
WD40
|
138 |
178 |
1.58e2 |
SMART |
WD40
|
181 |
228 |
4.26e1 |
SMART |
WD40
|
231 |
271 |
9.86e1 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000129132
|
SMART Domains |
Protein: ENSMUSP00000134935 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
48 |
88 |
8.55e-8 |
SMART |
Blast:WD40
|
91 |
131 |
1e-12 |
BLAST |
WD40
|
138 |
178 |
1.58e2 |
SMART |
WD40
|
181 |
228 |
4.26e1 |
SMART |
WD40
|
231 |
271 |
9.86e1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000144482
|
SMART Domains |
Protein: ENSMUSP00000134950 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
Blast:WD40
|
16 |
65 |
2e-24 |
BLAST |
WD40
|
70 |
109 |
1.59e-7 |
SMART |
WD40
|
112 |
152 |
2.39e0 |
SMART |
WD40
|
155 |
196 |
5.52e-2 |
SMART |
WD40
|
198 |
237 |
4.14e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000144711
|
SMART Domains |
Protein: ENSMUSP00000117710 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
72 |
112 |
8.55e-8 |
SMART |
WD40
|
194 |
235 |
7.64e1 |
SMART |
WD40
|
238 |
281 |
1.15e0 |
SMART |
WD40
|
366 |
405 |
1.59e-7 |
SMART |
WD40
|
408 |
448 |
2.39e0 |
SMART |
WD40
|
451 |
492 |
5.52e-2 |
SMART |
WD40
|
494 |
533 |
4.14e-6 |
SMART |
WD40
|
538 |
578 |
5.14e-11 |
SMART |
WD40
|
581 |
621 |
6.58e-9 |
SMART |
WD40
|
624 |
664 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000144711
|
SMART Domains |
Protein: ENSMUSP00000117710 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
72 |
112 |
8.55e-8 |
SMART |
WD40
|
194 |
235 |
7.64e1 |
SMART |
WD40
|
238 |
281 |
1.15e0 |
SMART |
WD40
|
366 |
405 |
1.59e-7 |
SMART |
WD40
|
408 |
448 |
2.39e0 |
SMART |
WD40
|
451 |
492 |
5.52e-2 |
SMART |
WD40
|
494 |
533 |
4.14e-6 |
SMART |
WD40
|
538 |
578 |
5.14e-11 |
SMART |
WD40
|
581 |
621 |
6.58e-9 |
SMART |
WD40
|
624 |
664 |
6.28e-6 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148806
|
Predicted Effect |
probably null
Transcript: ENSMUST00000150488
|
SMART Domains |
Protein: ENSMUSP00000122326 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
48 |
88 |
8.55e-8 |
SMART |
WD40
|
138 |
178 |
1.58e2 |
SMART |
WD40
|
181 |
228 |
4.26e1 |
SMART |
WD40
|
231 |
274 |
1.15e0 |
SMART |
WD40
|
359 |
398 |
1.59e-7 |
SMART |
WD40
|
401 |
441 |
2.39e0 |
SMART |
WD40
|
444 |
485 |
5.52e-2 |
SMART |
WD40
|
487 |
526 |
4.14e-6 |
SMART |
WD40
|
531 |
571 |
5.14e-11 |
SMART |
WD40
|
574 |
614 |
6.58e-9 |
SMART |
WD40
|
617 |
657 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000150488
|
SMART Domains |
Protein: ENSMUSP00000122326 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
48 |
88 |
8.55e-8 |
SMART |
WD40
|
138 |
178 |
1.58e2 |
SMART |
WD40
|
181 |
228 |
4.26e1 |
SMART |
WD40
|
231 |
274 |
1.15e0 |
SMART |
WD40
|
359 |
398 |
1.59e-7 |
SMART |
WD40
|
401 |
441 |
2.39e0 |
SMART |
WD40
|
444 |
485 |
5.52e-2 |
SMART |
WD40
|
487 |
526 |
4.14e-6 |
SMART |
WD40
|
531 |
571 |
5.14e-11 |
SMART |
WD40
|
574 |
614 |
6.58e-9 |
SMART |
WD40
|
617 |
657 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000175915
|
SMART Domains |
Protein: ENSMUSP00000135805 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
48 |
88 |
8.55e-8 |
SMART |
WD40
|
138 |
178 |
1.58e2 |
SMART |
WD40
|
181 |
228 |
4.26e1 |
SMART |
WD40
|
231 |
274 |
1.15e0 |
SMART |
WD40
|
359 |
398 |
1.59e-7 |
SMART |
WD40
|
401 |
441 |
2.39e0 |
SMART |
WD40
|
444 |
485 |
5.52e-2 |
SMART |
WD40
|
487 |
526 |
4.14e-6 |
SMART |
WD40
|
531 |
571 |
5.14e-11 |
SMART |
WD40
|
574 |
614 |
6.58e-9 |
SMART |
WD40
|
617 |
657 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000175915
|
SMART Domains |
Protein: ENSMUSP00000135805 Gene: ENSMUSG00000039375
Domain | Start | End | E-Value | Type |
WD40
|
48 |
88 |
8.55e-8 |
SMART |
WD40
|
138 |
178 |
1.58e2 |
SMART |
WD40
|
181 |
228 |
4.26e1 |
SMART |
WD40
|
231 |
274 |
1.15e0 |
SMART |
WD40
|
359 |
398 |
1.59e-7 |
SMART |
WD40
|
401 |
441 |
2.39e0 |
SMART |
WD40
|
444 |
485 |
5.52e-2 |
SMART |
WD40
|
487 |
526 |
4.14e-6 |
SMART |
WD40
|
531 |
571 |
5.14e-11 |
SMART |
WD40
|
574 |
614 |
6.58e-9 |
SMART |
WD40
|
617 |
657 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176866
|
Meta Mutation Damage Score |
0.9462 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 92.6%
|
Validation Efficiency |
100% (113/113) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a WD repeat-containing protein. It is abundantly expressed in retina and testis, and is thought to be a candidate gene for retinal disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2009]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
C |
T |
17: 24,593,274 (GRCm39) |
R224C |
probably damaging |
Het |
Adcy8 |
A |
T |
15: 64,659,207 (GRCm39) |
W528R |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 31,060,403 (GRCm39) |
R141Q |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,980,595 (GRCm39) |
H626Q |
probably benign |
Het |
Ampd2 |
A |
T |
3: 107,986,549 (GRCm39) |
M245K |
probably damaging |
Het |
Apob |
G |
A |
12: 8,055,219 (GRCm39) |
|
probably null |
Het |
Apool |
C |
T |
X: 111,259,540 (GRCm39) |
Q60* |
probably null |
Het |
Aqp1 |
A |
T |
6: 55,322,520 (GRCm39) |
I172F |
probably damaging |
Het |
Atp7a |
A |
G |
X: 105,153,374 (GRCm39) |
D1092G |
probably benign |
Het |
Bcas3 |
A |
G |
11: 85,261,958 (GRCm39) |
Y110C |
probably damaging |
Het |
Brpf1 |
T |
C |
6: 113,287,215 (GRCm39) |
S148P |
probably damaging |
Het |
Capn3 |
A |
G |
2: 120,322,301 (GRCm39) |
H339R |
probably damaging |
Het |
Ccdc141 |
A |
T |
2: 76,954,722 (GRCm39) |
|
probably null |
Het |
Ccl2 |
A |
G |
11: 81,927,984 (GRCm39) |
|
probably benign |
Het |
Cct8l1 |
G |
A |
5: 25,721,881 (GRCm39) |
V199I |
probably benign |
Het |
Cdc23 |
C |
A |
18: 34,784,742 (GRCm39) |
V7L |
unknown |
Het |
Cit |
T |
A |
5: 116,084,902 (GRCm39) |
M811K |
probably benign |
Het |
Crim1 |
T |
C |
17: 78,588,776 (GRCm39) |
C284R |
possibly damaging |
Het |
Cyp2d10 |
C |
T |
15: 82,287,954 (GRCm39) |
R383H |
probably benign |
Het |
Cyp4a29 |
A |
G |
4: 115,104,860 (GRCm39) |
T123A |
probably benign |
Het |
Dbndd2 |
A |
G |
2: 164,332,224 (GRCm39) |
|
probably benign |
Het |
Dnaja3 |
A |
T |
16: 4,514,289 (GRCm39) |
T274S |
probably damaging |
Het |
Dot1l |
A |
G |
10: 80,620,480 (GRCm39) |
D514G |
possibly damaging |
Het |
Dysf |
A |
T |
6: 84,114,254 (GRCm39) |
K1226M |
probably damaging |
Het |
Eef1akmt1 |
A |
G |
14: 57,803,464 (GRCm39) |
L30P |
probably damaging |
Het |
Elavl1 |
A |
G |
8: 4,351,741 (GRCm39) |
M125T |
possibly damaging |
Het |
Eml4 |
C |
A |
17: 83,771,006 (GRCm39) |
S723R |
probably damaging |
Het |
Fgf15 |
A |
C |
7: 144,450,576 (GRCm39) |
Y54S |
possibly damaging |
Het |
Fign |
A |
T |
2: 63,810,037 (GRCm39) |
L411* |
probably null |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Fryl |
G |
A |
5: 73,232,110 (GRCm39) |
P1550L |
probably damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gprasp2 |
C |
T |
X: 134,743,346 (GRCm39) |
T235I |
possibly damaging |
Het |
H2ab3 |
T |
C |
X: 119,222,543 (GRCm39) |
T84A |
probably damaging |
Het |
Hal |
A |
T |
10: 93,349,904 (GRCm39) |
I555F |
probably damaging |
Het |
Hdac6 |
A |
G |
X: 7,811,036 (GRCm39) |
F104L |
probably damaging |
Het |
Hibadh |
C |
T |
6: 52,597,079 (GRCm39) |
V122M |
possibly damaging |
Het |
Hmga1b |
C |
T |
11: 120,654,012 (GRCm39) |
Q100* |
probably null |
Het |
Hydin |
A |
G |
8: 111,265,105 (GRCm39) |
N2763D |
probably benign |
Het |
Ifi47 |
A |
G |
11: 48,986,361 (GRCm39) |
T43A |
probably benign |
Het |
Ifnlr1 |
A |
G |
4: 135,432,457 (GRCm39) |
T298A |
probably benign |
Het |
Impdh2 |
G |
A |
9: 108,440,535 (GRCm39) |
|
probably null |
Het |
Insr |
A |
G |
8: 3,209,475 (GRCm39) |
F1203L |
probably damaging |
Het |
Kcnq4 |
A |
G |
4: 120,574,714 (GRCm39) |
S117P |
probably damaging |
Het |
Kif19a |
G |
A |
11: 114,658,053 (GRCm39) |
M37I |
probably benign |
Het |
Kif1a |
T |
C |
1: 92,950,227 (GRCm39) |
H1400R |
probably damaging |
Het |
Kiss1r |
C |
A |
10: 79,754,596 (GRCm39) |
S30* |
probably null |
Het |
Krt222 |
T |
A |
11: 99,134,796 (GRCm39) |
|
probably benign |
Het |
Lekr1 |
A |
T |
3: 65,727,215 (GRCm39) |
|
noncoding transcript |
Het |
Ltn1 |
A |
G |
16: 87,224,628 (GRCm39) |
V32A |
probably damaging |
Het |
Marchf1 |
T |
A |
8: 66,839,020 (GRCm39) |
W21R |
probably benign |
Het |
Marchf5 |
A |
G |
19: 37,188,207 (GRCm39) |
N58S |
possibly damaging |
Het |
Mast4 |
G |
A |
13: 102,875,391 (GRCm39) |
Q1158* |
probably null |
Het |
Mib2 |
C |
G |
4: 155,741,233 (GRCm39) |
A535P |
probably damaging |
Het |
Mrtfa |
A |
G |
15: 80,906,627 (GRCm39) |
V91A |
probably damaging |
Het |
Msc |
C |
T |
1: 14,824,537 (GRCm39) |
V178M |
probably benign |
Het |
Muc4 |
C |
A |
16: 32,754,529 (GRCm38) |
H1468N |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,412,999 (GRCm39) |
T1982S |
unknown |
Het |
Mvk |
A |
T |
5: 114,591,013 (GRCm39) |
|
probably benign |
Het |
Myo1a |
T |
C |
10: 127,543,288 (GRCm39) |
|
probably null |
Het |
Myo6 |
T |
G |
9: 80,195,290 (GRCm39) |
S887A |
probably benign |
Het |
Myo7a |
G |
A |
7: 97,722,425 (GRCm39) |
Q1167* |
probably null |
Het |
Ncald |
A |
T |
15: 37,397,478 (GRCm39) |
H67Q |
probably damaging |
Het |
Nmnat1 |
C |
A |
4: 149,553,595 (GRCm39) |
M172I |
probably benign |
Het |
Nudt1 |
G |
T |
5: 140,317,662 (GRCm39) |
|
probably null |
Het |
Nudt5 |
T |
A |
2: 5,869,198 (GRCm39) |
H141Q |
probably benign |
Het |
Or1m1 |
T |
C |
9: 18,666,118 (GRCm39) |
E271G |
possibly damaging |
Het |
Or4e1 |
T |
A |
14: 52,701,032 (GRCm39) |
M118L |
probably damaging |
Het |
Or8h10 |
A |
T |
2: 86,808,666 (GRCm39) |
V158D |
possibly damaging |
Het |
Parp14 |
A |
T |
16: 35,655,077 (GRCm39) |
I1798K |
probably damaging |
Het |
Pcdhga7 |
A |
G |
18: 37,849,025 (GRCm39) |
D344G |
probably damaging |
Het |
Pck1 |
A |
G |
2: 172,998,770 (GRCm39) |
T343A |
probably benign |
Het |
Pik3c2g |
T |
A |
6: 139,665,873 (GRCm39) |
C65S |
probably null |
Het |
Pilra |
A |
G |
5: 137,833,674 (GRCm39) |
F131L |
probably damaging |
Het |
Ppl |
A |
T |
16: 4,906,742 (GRCm39) |
S1184R |
probably benign |
Het |
Prmt2 |
C |
T |
10: 76,058,390 (GRCm39) |
V140I |
probably damaging |
Het |
Prpf38b |
A |
G |
3: 108,818,484 (GRCm39) |
F92S |
probably damaging |
Het |
Psmc3 |
A |
G |
2: 90,884,915 (GRCm39) |
|
probably benign |
Het |
Ptgs1 |
A |
T |
2: 36,141,272 (GRCm39) |
N573I |
probably damaging |
Het |
Rgs9 |
C |
A |
11: 109,118,157 (GRCm39) |
A332S |
probably benign |
Het |
Rptor |
T |
C |
11: 119,787,305 (GRCm39) |
I1290T |
possibly damaging |
Het |
Slc38a7 |
C |
A |
8: 96,568,278 (GRCm39) |
R369L |
probably damaging |
Het |
Slc4a2 |
G |
A |
5: 24,643,760 (GRCm39) |
S855N |
probably benign |
Het |
Slco2a1 |
G |
T |
9: 102,923,925 (GRCm39) |
L46F |
probably damaging |
Het |
Snrpd3 |
G |
T |
10: 75,355,227 (GRCm39) |
C20F |
possibly damaging |
Het |
Stab2 |
A |
T |
10: 86,699,422 (GRCm39) |
I481N |
probably benign |
Het |
Tbc1d9 |
A |
G |
8: 83,960,176 (GRCm39) |
E143G |
probably damaging |
Het |
Tenm2 |
T |
A |
11: 35,959,208 (GRCm39) |
T1114S |
probably damaging |
Het |
Tg |
A |
C |
15: 66,607,101 (GRCm39) |
M213L |
probably benign |
Het |
Tnc |
A |
G |
4: 63,938,648 (GRCm39) |
C64R |
probably damaging |
Het |
Tpd52l1 |
A |
G |
10: 31,233,916 (GRCm39) |
L79S |
probably damaging |
Het |
Tpp2 |
C |
A |
1: 43,993,896 (GRCm39) |
S260R |
possibly damaging |
Het |
Tppp2 |
G |
A |
14: 52,157,912 (GRCm39) |
R119Q |
probably benign |
Het |
Tshz2 |
A |
T |
2: 169,804,493 (GRCm39) |
|
probably benign |
Het |
Tuba8 |
T |
C |
6: 121,199,862 (GRCm39) |
V182A |
probably damaging |
Het |
Ufl1 |
A |
G |
4: 25,254,780 (GRCm39) |
Y559H |
probably benign |
Het |
Usp53 |
A |
T |
3: 122,727,595 (GRCm39) |
S996T |
probably benign |
Het |
Vcam1 |
A |
G |
3: 115,918,037 (GRCm39) |
V308A |
probably damaging |
Het |
Wdr6 |
G |
A |
9: 108,451,565 (GRCm39) |
H773Y |
probably damaging |
Het |
Wnk4 |
T |
G |
11: 101,152,014 (GRCm39) |
F173V |
probably damaging |
Het |
Xrcc5 |
T |
C |
1: 72,378,188 (GRCm39) |
Y395H |
probably damaging |
Het |
Zcwpw1 |
T |
A |
5: 137,793,781 (GRCm39) |
M1K |
probably null |
Het |
Zfp263 |
A |
G |
16: 3,564,704 (GRCm39) |
R240G |
possibly damaging |
Het |
Zfp652 |
A |
G |
11: 95,640,890 (GRCm39) |
I272V |
possibly damaging |
Het |
|
Other mutations in Wdr17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00309:Wdr17
|
APN |
8 |
55,140,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00496:Wdr17
|
APN |
8 |
55,112,614 (GRCm39) |
splice site |
probably benign |
|
IGL01318:Wdr17
|
APN |
8 |
55,125,585 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01347:Wdr17
|
APN |
8 |
55,104,380 (GRCm39) |
missense |
probably benign |
|
IGL01654:Wdr17
|
APN |
8 |
55,115,914 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02010:Wdr17
|
APN |
8 |
55,112,738 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02085:Wdr17
|
APN |
8 |
55,140,771 (GRCm39) |
nonsense |
probably null |
|
IGL02205:Wdr17
|
APN |
8 |
55,149,335 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02375:Wdr17
|
APN |
8 |
55,149,423 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02705:Wdr17
|
APN |
8 |
55,101,250 (GRCm39) |
splice site |
probably null |
|
IGL02719:Wdr17
|
APN |
8 |
55,146,089 (GRCm39) |
splice site |
probably null |
|
IGL03051:Wdr17
|
APN |
8 |
55,104,349 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03131:Wdr17
|
APN |
8 |
55,149,302 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03172:Wdr17
|
APN |
8 |
55,114,515 (GRCm39) |
missense |
probably damaging |
0.96 |
enthralled
|
UTSW |
8 |
55,112,716 (GRCm39) |
missense |
possibly damaging |
0.85 |
riveted
|
UTSW |
8 |
55,085,522 (GRCm39) |
missense |
probably benign |
0.00 |
thrilled
|
UTSW |
8 |
55,149,303 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03138:Wdr17
|
UTSW |
8 |
55,102,178 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4458001:Wdr17
|
UTSW |
8 |
55,126,614 (GRCm39) |
nonsense |
probably null |
|
R0011:Wdr17
|
UTSW |
8 |
55,125,536 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0011:Wdr17
|
UTSW |
8 |
55,125,536 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0124:Wdr17
|
UTSW |
8 |
55,088,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Wdr17
|
UTSW |
8 |
55,116,043 (GRCm39) |
missense |
probably benign |
0.08 |
R0270:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0271:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0288:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0321:Wdr17
|
UTSW |
8 |
55,149,303 (GRCm39) |
critical splice donor site |
probably null |
|
R0464:Wdr17
|
UTSW |
8 |
55,123,427 (GRCm39) |
splice site |
probably benign |
|
R0479:Wdr17
|
UTSW |
8 |
55,104,456 (GRCm39) |
splice site |
probably null |
|
R0488:Wdr17
|
UTSW |
8 |
55,146,087 (GRCm39) |
unclassified |
probably benign |
|
R0552:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0553:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0600:Wdr17
|
UTSW |
8 |
55,114,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R0621:Wdr17
|
UTSW |
8 |
55,096,226 (GRCm39) |
missense |
probably benign |
0.18 |
R0655:Wdr17
|
UTSW |
8 |
55,102,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0789:Wdr17
|
UTSW |
8 |
55,112,607 (GRCm39) |
splice site |
probably benign |
|
R0854:Wdr17
|
UTSW |
8 |
55,156,916 (GRCm39) |
missense |
probably benign |
|
R0879:Wdr17
|
UTSW |
8 |
55,114,516 (GRCm39) |
missense |
probably benign |
0.08 |
R1462:Wdr17
|
UTSW |
8 |
55,123,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Wdr17
|
UTSW |
8 |
55,123,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1497:Wdr17
|
UTSW |
8 |
55,125,536 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1589:Wdr17
|
UTSW |
8 |
55,156,942 (GRCm39) |
intron |
probably benign |
|
R1618:Wdr17
|
UTSW |
8 |
55,092,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Wdr17
|
UTSW |
8 |
55,126,689 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1778:Wdr17
|
UTSW |
8 |
55,143,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1819:Wdr17
|
UTSW |
8 |
55,143,159 (GRCm39) |
missense |
probably benign |
0.18 |
R1913:Wdr17
|
UTSW |
8 |
55,140,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Wdr17
|
UTSW |
8 |
55,085,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Wdr17
|
UTSW |
8 |
55,125,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R2309:Wdr17
|
UTSW |
8 |
55,096,283 (GRCm39) |
missense |
probably benign |
|
R3882:Wdr17
|
UTSW |
8 |
55,092,536 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4097:Wdr17
|
UTSW |
8 |
55,088,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R4372:Wdr17
|
UTSW |
8 |
55,092,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R4380:Wdr17
|
UTSW |
8 |
55,101,442 (GRCm39) |
intron |
probably benign |
|
R4480:Wdr17
|
UTSW |
8 |
55,117,999 (GRCm39) |
critical splice donor site |
probably null |
|
R4654:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R4656:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R4669:Wdr17
|
UTSW |
8 |
55,143,083 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4719:Wdr17
|
UTSW |
8 |
55,092,911 (GRCm39) |
missense |
probably benign |
0.33 |
R4912:Wdr17
|
UTSW |
8 |
55,082,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Wdr17
|
UTSW |
8 |
55,118,161 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5176:Wdr17
|
UTSW |
8 |
55,106,913 (GRCm39) |
critical splice donor site |
probably null |
|
R5194:Wdr17
|
UTSW |
8 |
55,140,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5270:Wdr17
|
UTSW |
8 |
55,096,221 (GRCm39) |
missense |
probably benign |
0.20 |
R5300:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5325:Wdr17
|
UTSW |
8 |
55,112,716 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5336:Wdr17
|
UTSW |
8 |
55,085,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5394:Wdr17
|
UTSW |
8 |
55,092,524 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5424:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5425:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5426:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5548:Wdr17
|
UTSW |
8 |
55,156,886 (GRCm39) |
missense |
probably damaging |
0.97 |
R5681:Wdr17
|
UTSW |
8 |
55,115,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5722:Wdr17
|
UTSW |
8 |
55,113,806 (GRCm39) |
critical splice donor site |
probably null |
|
R5894:Wdr17
|
UTSW |
8 |
55,149,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R5906:Wdr17
|
UTSW |
8 |
55,092,503 (GRCm39) |
missense |
probably benign |
0.33 |
R6038:Wdr17
|
UTSW |
8 |
55,085,346 (GRCm39) |
critical splice donor site |
probably null |
|
R6038:Wdr17
|
UTSW |
8 |
55,085,346 (GRCm39) |
critical splice donor site |
probably null |
|
R6391:Wdr17
|
UTSW |
8 |
55,114,495 (GRCm39) |
missense |
probably benign |
0.04 |
R6605:Wdr17
|
UTSW |
8 |
55,134,559 (GRCm39) |
missense |
probably benign |
0.16 |
R6892:Wdr17
|
UTSW |
8 |
55,126,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Wdr17
|
UTSW |
8 |
55,134,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Wdr17
|
UTSW |
8 |
55,085,522 (GRCm39) |
missense |
probably benign |
0.00 |
R7481:Wdr17
|
UTSW |
8 |
55,114,371 (GRCm39) |
missense |
probably benign |
|
R7868:Wdr17
|
UTSW |
8 |
55,149,302 (GRCm39) |
critical splice donor site |
probably null |
|
R7939:Wdr17
|
UTSW |
8 |
55,140,677 (GRCm39) |
missense |
probably damaging |
0.98 |
R7962:Wdr17
|
UTSW |
8 |
55,113,806 (GRCm39) |
critical splice donor site |
probably null |
|
R8017:Wdr17
|
UTSW |
8 |
55,091,403 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8122:Wdr17
|
UTSW |
8 |
55,118,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8226:Wdr17
|
UTSW |
8 |
55,146,155 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8251:Wdr17
|
UTSW |
8 |
55,110,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R8413:Wdr17
|
UTSW |
8 |
55,115,953 (GRCm39) |
missense |
probably benign |
0.08 |
R8534:Wdr17
|
UTSW |
8 |
55,101,265 (GRCm39) |
missense |
probably benign |
0.08 |
R8708:Wdr17
|
UTSW |
8 |
55,093,127 (GRCm39) |
intron |
probably benign |
|
R9116:Wdr17
|
UTSW |
8 |
55,114,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R9258:Wdr17
|
UTSW |
8 |
55,112,654 (GRCm39) |
nonsense |
probably null |
|
R9351:Wdr17
|
UTSW |
8 |
55,143,057 (GRCm39) |
missense |
probably benign |
0.00 |
R9475:Wdr17
|
UTSW |
8 |
55,088,512 (GRCm39) |
missense |
probably benign |
0.00 |
R9546:Wdr17
|
UTSW |
8 |
55,112,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R9547:Wdr17
|
UTSW |
8 |
55,112,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R9635:Wdr17
|
UTSW |
8 |
55,101,375 (GRCm39) |
missense |
probably damaging |
0.98 |
V5088:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
V5622:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
V5622:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
X0022:Wdr17
|
UTSW |
8 |
55,092,529 (GRCm39) |
missense |
probably benign |
0.04 |
X0066:Wdr17
|
UTSW |
8 |
55,126,595 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Wdr17
|
UTSW |
8 |
55,123,414 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Wdr17
|
UTSW |
8 |
55,096,220 (GRCm39) |
missense |
probably benign |
0.03 |
|
Predicted Primers |
PCR Primer
(F):5'- GTGTGCCACCTAAATATGCAAATG -3'
(R):5'- AAAGGTATCACCAGGTCTACACCG -3'
Sequencing Primer
(F):5'- GTCAGACGCAAAACTATGGGCTTC -3'
(R):5'- GGTCTACACCGTAGCATAATGAG -3'
|
Posted On |
2016-06-06 |